A modular tool to aggregate results from bioinformatics analyses across many samples into a single report.
/home/samson/projects/RESPONSIBILIES_TRAINING/project/nf_python_demo/nf_python_variant_splitter/R1_batch_variant_splitter_nextflow/results_user
R1 Variant Splitter — variant summary
SNV/INDEL counts per sample (from bcftools outputs).
| Sample | snvs | indels |
|---|---|---|
| father | 5024 | 722 |
| mother | 4891 | 662 |
| proband | 5292 | 742 |